Flexible RF ablation needle

ABSTRACT

Embodiments disclosed herein are directed to devices, methods, and systems for the treatment of tissue using energy delivery. Specifically, certain embodiments may be used for the treatment of lung tissue, such as lung nodules, using RF ablation, via a catheter provided with a first electrode attached to a distal end of the catheter, wherein the first electrode is hollow, wherein the first electrode comprises a piercing tip configured to pierce through an airway all and a second electrode received in a movable manner within the first electrode, wherein the second electrode is extendable from the first electrode to form a first extended configuration.

CROSS REFERENCE TO RELATED APPLICATIONS

This application claims priority to and the benefit of U.S. provisionalpatent application Ser. No. 61/785,888 filed on Mar. 14, 2013 entitled“Flexible RF Ablation Needle,” the entire disclosure of which is herebyincorporated by reference as if set forth in its entirety for allpurposes.

BACKGROUND

1. Technical Field

The present invention generally relates to the treatment of tissue viaenergy delivery. More particularly, certain embodiments of the presentinvention relate to thermal ablation of lung tissue with energydelivered via a piercing needle.

2. Description of the Related Art

Lung cancer has a high incidence of morbidity and mortality in patients.Early stages of lung cancer can take the form of pulmonary nodules (inparticular those under between 0.5 mm and 30 mm in size) and may requirecareful evaluation by a medical professional, especially in patientsthat have risk factors such as tobacco use or a family history ofcancer.

Lung nodules, lesions, tumors, and other cancerous or pre-cancerousregions of tissue in the lung, may be difficult to treat with invasivesurgical techniques, with attendant complications such as excessivebleeding, infection risk, air leaks, pneumothorax, and other suchissues. In particular, regions deep in the lung may be difficult toaccess using conventional methods, further increasing the difficulty oftreatment.

Electrical ablation, in particular radiofrequency electrical ablation,has been used in the treatment of tumors and other masses present insolid tissues such as the liver. Use of such techniques in the lungs,however, entails some attendant complications and difficulties. First,the use of conventional electrical ablation probes requires piercinginto the thoracic cavity and into the lung, with a consequent highlikelihood of pneumothorax, excessive bleeding and other complications.Moreover, these transthoracic ablation probes are rigid and may not beable to reach certain areas of the pulmonary anatomy.

While there have been some attempts to pursue radiofrequency electricalablation via bronchoscopes inserted into airways, these attempts arelimited by the confines of the airway passage and the reach of thebronchoscope—which cannot enter into very small peripheral lungpassages—and accordingly may not be able to position the probes ardordeliver sufficient energy to treat tissue such as lung nodulesadequately. Damage to the airway itself may result from the treatmentprocess. Additionally, it will be noted that visualization andlocalization of the tissue region to be treated may present challenges,especially for tissue regions deep in the lung.

SUMMARY

It is therefore a goal of the embodiments described herein to providenew devices, systems, and methods for the treatment of tissue, inparticular lung tissue and lung nodules.

In a first embodiment, a device for the delivery of energy to a regionof lung tissue, the device comprises:

-   -   a catheter configured to be inserted into an airway;    -   a first electrode attached to the distal end of the catheter,        wherein the first electrode is hollow, wherein the first        electrode comprises a piercing, tip configured to pierce through        an airway wall;    -   a second electrode received in a movable manner within the first        electrode, wherein the second electrode is extendable from a        distal end of the first electrode to form a first extended        configuration;    -   a handle attached at a proximal end of the catheter, wherein the        handle comprises a second activation toggle configured to extend        the second electrode from the first electrode; and    -   a first electrical lead in electric communication with the first        electrode, and a second electrical lead in electric        communication with the second electrode, wherein the first and        second electrical leads are connectable to a source of electric        power.

In some embodiments, the catheter is dimensioned to be insertable into abronchoscope. In some embodiments, the bronchoscope comprises aside-facing ultrasound probe. Preferably, the first electrode may beflexible. In some embodiments, the first electrode may be bendable to anangle of at least 10° relative to a first longitudinal axis definedrelative to the longitudinal axis of the axial length of the airway. Ina further embodiment, the second electrode, when in a first extendedconfiguration, forms a coil. In some embodiments, the coil is configuredto corkscrew into at least part of the region of lung tissue. Furtherembodiments may comprise the second electrode being constructed at leastin part from a shape-memory material having a martensite configurationat a first lower temperature, and an austenite configuration at a secondtemperature above body temperature, and wherein the second electrode isconfigured to adopt a first straight configuration while in themartensite configuration, and a bend or coil while in the austeniteconfiguration. The second electrode may adopt the austeniteconfiguration when in the first extended configuration.

In some embodiments, the handle further comprises a first activationtoggle configured to extend the first electrode. In some embodiments,the second activation toggle is connected to the first activationtoggle, and wherein the first and second electrodes are flexible andconnect the second activation toggle to the first activation toggle. Ina further embodiment, the second activation toggle comprises a movablegrip configured to move in a longitudinal axial direction with respectto a static grip. The second activation toggle may be configured todeploy the second electrode when the movable grip is moved in alongitudinal axial direction with respect to the static grip.

In some embodiments, the handle further comprises a bronchoscopeattachment configured to attach to the working channel of abronchoscope. Preferably, the bronchoscope attachment may comprise abronchoscope guide configured to be inserted at least partially into theworking channel of the bronchoscope. In some embodiments, the cathetermay further comprise a guide sheath disposed over at least a portion ofthe catheter shaft. Preferably, the source of electric power comprises aradiofrequency generator. The first and second electrodes may comprise abipolar radiofrequency ablation electrode.

Some embodiments further comprise a fluid source connected to thecatheter and in fluid communication with at least one of the first orsecond electrodes. In some embodiments, the fluid source is configuredto flow out of the first electrode. The catheter may comprise a fluidinjection port configured to be attached to the fluid source. The fluidsource may comprise a saline solution. The fluid source may comprise avisualization agent. The fluid source may comprise a medicant. In someembodiments, the fluid source circulates within one or both of the firstand second electrodes without flowing out of the first and secondelectrodes.

In some embodiments, the device further comprises an impedance detectorattached to one or more of the first and second electrodes, theimpedance detector configured to detect the impedance of the surroundingtissue. The device may further comprise a temperature sensor configuredto detect the temperature of the surrounding tissue. The temperaturesensor may be attached or integrated to one or more of the first andsecond electrodes. The temperature sensor may be separate from the firstand second electrodes. Some embodiments further comprise a feedbackmechanism configured to change the amount of power applied to the tissuein response to one or more monitored attributes. The one or moremonitored attributes may be selected from the group consisting of tissuetemperature, tissue impedance, amount of fluid delivered, energy, andtime. In some embodiments, the feedback mechanism is configured to stopthe application of power applied to the tissue in response to a level ofthe one or more monitored attributes exceeding a predetermined limit.

In a second embodiment, a method of delivering energy to a region oflung tissue to be treated, the method comprises:

-   -   inserting a catheter into a patient's airway, wherein the distal        end of the catheter comprises a first electrode and a second        electrode received in a sliding manner within the first        electrode and configured to be extendable therefrom;    -   navigating the catheter to an airway proximate the region of        lung tissue to be treated;    -   piercing the airway with the first electrode so as to position        the first electrode into or near the region of lung tissue to be        treated;    -   extending the second electrode into the region of lung tissue to        be treated;    -   activating a power source configured to deliver a therapeutic        amount of energy to the region of lung tissue to be treated,        wherein the power source is connected via a first electrical        lead connected to the first electrode and a second electrical        lead connected to the second electrode; and    -   delivering energy to the region of lung tissue to be treated.

In some embodiments, the energy delivered to the region of lung tissuecomprises radiofrequency ablation. Some embodiments further comprisebending at least the first electrode at an angle relative to andnon-parallel to a first longitudinal axis defined relative to the axiallength of the catheter. Some embodiments further comprise inserting thecatheter into a bronchoscope, the bronchoscope being inserted into thepatient airway. In some embodiments, the bronchoscope comprises anultrasound sensor, and wherein the ultrasound sensor is used to navigatethe catheter. In some embodiments, the ultrasound sensor faces at adirection perpendicular the first longitudinal axis. The catheter may benavigated to the region of lung tissue to be treated by one or moremethods selected from the group consisting of fluoroscopy and real-timecomputerized tomography. Some embodiments further comprise monitoring atleast one monitored attribute associated with the delivery of energy tothe region of lung tissue to be treated. In some embodiments, the atleast one monitored attribute is selected from the group consisting oftissue temperature, tissue impedance, and time. Some embodiments furthercomprise changing the amount of power delivered by the power source inresponse to a feedback mechanism responsive to at least one monitoredattribute. Some embodiments further comprise stopping the application ofpower applied to the tissue in response to a level of the one or moremonitored attribute exceeding a predetermined limit.

In another embodiment, a system for the delivery of energy to a regionof lung tissue, the system comprises: an energy delivery devicecomprising: a catheter configured to be inserted into an airway, thecatheter comprising a first electrode and a second electrode; a handleattached at a proximal end of the catheter, the handle comprising asecond activation toggle configured to extend the second electrode fromthe first electrode; wherein the second electrode is received in amovable manner within the first electrode, and wherein the secondelectrode is extendable from a distal end of the first electrode to forma first extended configuration; a power source connected to the firstelectrode and second electrode via first and second electrical leads,the power source configured to deliver RF energy; and a conduitinsertable into an airway and selected from the group consisting of abronchoscope and guide sheath, the catheter being insertable and movabletherein.

In some embodiments, the system further comprises a fluid sourceconnected to the device and configured to deliver fluid out of a distalend of the catheter. Some embodiments may comprise one or moreadditional sensors configured to monitor one or more monitoredattributes of the system, wherein the one or more monitored attributesare selected from the group consisting of: temperature, electricalparameters, and fluid flow rate. Some embodiments further comprise afeedback system responsive to at least one of the monitored attributes,wherein the feedback system is configured to change or stop one or moretreatment attributes.

BRIEF DESCRIPTION OF THE DRAWINGS

These and other features, aspects and advantages of the presentdisclosure will now be described with reference to several drawings,which drawings are intended to be illustrative and not limiting.

FIG. 1 illustrates an embodiment of a catheter that is arranged andconfigured in accordance with certain features, aspects and advantagesof an embodiment of the present disclosure.

FIG. 2 illustrates the catheter of FIG. 1 being inserted through abronchoscope and into an airway.

FIGS. 3A and 3B illustrate two electrodes of the catheter of FIG. 1 inan undeployed and deployed position, respectively.

FIG. 3C illustrates a distal end of a catheter having two electrodes.

FIG. 3D illustrates a distal end of a catheter having two electrodeswherein one electrode wraps around the other.

FIG. 3E illustrates a distal end of a catheter having two electrodeswherein one electrode spans an aperture in the catheter wall.

FIG. 3F illustrates a distal end of a catheter having two electrodeswherein one electrode wraps around the other and is attached to leadsexternal to the catheter.

FIG. 3G illustrates a distal end of a catheter having two electrodesdeployed through the wall of an airway or other body lumen.

FIG. 4 is a view of the catheter of FIG. 1 deployed through an airway inconjunction with a bronchoscope containing an ultrasound probe.

FIG. 5 is a detail of a handle portion of the catheter of FIG. 1.

FIGS. 6A-6C illustrate deployment steps of the catheter of FIG. 1.

FIG. 7 is a detail of a fluid infusion port that may be present in thecatheter of FIG. 1.

FIGS. 8A-8D illustrate another embodiment of a handle portion of acatheter that is arranged and configured in accordance with certainfeatures, aspects and advantages of an embodiment of the presentdisclosure.

FIG. 8E illustrates another embodiment of a handle portion of a catheterthat is arranged and configured in accordance with certain features,aspects and advantages of the present disclosure.

FIG. 9 is a close-up of the distal tip of a catheter, illustrating asaline solution being dispensed therefrom.

FIG. 10 illustrate embodiments of different electrode types that may beused in conjunction with the catheters described herein.

DETAILED DESCRIPTION

Embodiments of an apparatus, system and method for identification andtreatment of regions of the lung, and in particular, pulmonary nodulesand lesions, will be described with reference to the accompanyingfigures of one or more embodiments. The terminology used in thedescription presented herein is not intended to be interpreted in anylimited or restrictive manner. Rather, the terminology is simply beingutilized in conjunction with a detailed description of embodiments ofthe systems, methods and related components. Furthermore, embodimentsmay comprise several novel features, no single one of which is solelyresponsible for its desirable attributes or is believed to be essentialto practicing the inventions herein described.

The terms “lung region,” “lung area,” “tissue,” “lesion” and “nodule” asused herein are broad interchangeable terms and, unless otherwiseindicated or apparent from the context of use, the terms can includewithin their meaning, and without limitation, other organs or regions oftissue in a human or animal body, including diseased, cancerous, and/orpre-cancerous tissue, as well as tissue showing lesions, or generallyany tissue region for which treatment is desired. Although someembodiments described herein refer to identifying and treating an areawithin a lung, this disclosure is not so limited, and the embodimentsdescribed herein may be used in other vessels, passages, body cavities,and organs in humans and animals. For example, the methods andapparatuses described herein can be used to treat abdominal organs,lymphatic system, prostate, urinary tract (including bladder), genitalorgans, breasts and/or other areas/systems of the body.

FIG. 1 illustrates an embodiment of a catheter system 100 that isarranged and configured in accordance with certain features, aspects andadvantages of the present invention. The illustrated catheter system 100comprises a catheter shaft 101 connected to a handle 120. The handle 120preferably is configured to be gripped by one hand of a user (e.g., adoctor, nurse, or other health professional).

The handle 120 may comprise a thumb pad 121. The thumb pad 121 mayprovide additional support when the handle 120 is being held. One ormore surfaces of the handle 120 also may be designed to be grippable. Insome configurations, at least a portion of the grippable portions of thehandle 120 may comprise knurling, rubberized surfaces or the like toimprove the ability to maintain a grip on the handle 120, for examplebut without limitations.

In some configurations, the thumb pad 121 may be connected to, orotherwise act as, a clamp. For example, the clamp can be used tomaintain a position of the catheter shaft 101 relative to the handle120. For example, the thumb pad 121 may be configured with a twistingscrew engagement that allows a portion of the handle 120 to clamp ontothe catheter shaft 101, which can extend at least partially through thehandle 120. Other configurations also can be used to secure the cathetershaft 101 in position relative to the handle 120.

The catheter shaft 101 can be connected at its proximal end 110 to thehandle 120. As will be explained in greater detail below, the cathetershaft 101 may have a first electrode 103 at a distal end 109 of thecatheter shaft 101. In some configurations, the catheter shaft 101 cancomprise a second electrode 105. The second electrode 105 can be movablerelative to the first electrode 103. In some configurations, the secondelectrode 105 can be received in a movable mariner within the firstelectrode 103. In some configurations, the second electrode 105 can beextendible from the first electrode 103.

As will be discussed below, a first electrode 103 and a second electrode105 can be electrically connected to a first electrical lead 107 and asecond electrical lead 108, respectively. The electrical lead 107 can beon an opposite side of a fluid port 830 relative to a first electricaltoggle 124. The first electrical lead 107 is visible in FIG. 7.

As shown in FIG. 2, a power source 112 may be connected to the first andsecond electrical leads 107, 108, for example via wires and the like. Assuch, the power source 112 can deliver power to the first electrode 103and/or the second electrode 105 through the first and second electricalleads 107, 108. Thus, the power source 112 can be configured to deliverenergy to a region of tissue via the catheter system 100, which includesone or more of the first and second electrodes 103, 105.

In some configurations, the power source 112 comprises a source ofelectric or electromagnetic power. Other sources of energy, alone or incombination, can be used and energy can be delivered to the tissue viathe power source 112 and/or the catheter system 100. Such power sourcescan include direct current treatment, cryo treatment (includingcryoablation), microwave, laser, and/or photodynamic treatment, forexample but without limitation.

In some configurations, the power source 112 may be configured todeliver electric power at varied frequencies. In some configurations,the power source 112 can be configured to deliver radiofrequency (“RF”)energy in a range of between about 3 KHz and about 300 GHz. In someconfigurations, the power range is between about 100 KHz and about 500KHz. In some configurations, the power range is between about 300 KHzand about 400 KHz.

In some configurations, the power source 112 can deliver power in arange of between about 5 watts and about 40 watts. For some therapeutictreatments, the range can be between about 7 watts and about 25 watts.In some configurations, the range can be between about 8 watts and about13 watts.

In some configurations, the power level can be set by the user oroperator, and the resulting voltage and current will vary in accordancewith that setting. In some configurations, the voltage and the currentcan vary between the ranges of about 20 VAC and about 60 VAC and betweenabout 0.1 ampere and about 1 amperes.

In some configurations, the energy delivered to a 1 cm diameter volumetreatment site is between about 8 KJ and about 13 KJ, depending upon thetissue type. As explained below in greater detail, the energy deliveredto the tissue affects the tissue ablation area.

In some configurations, the system 100 acts to heat or ablate tissue viaRF energy, although such treatment is also possible by using otherenergy delivery techniques. In particular, tissue such as tumors(especially lung nodules) or other tissue masses may be treated withenergy so as to heat the cells therein to ablate, kill, burn, heat, ordenature the cells. The tissue may not necessarily need to be heated soas to kill the component cells, but may be heated enough to modify thecells so as to become non-malignant or otherwise benign. As describedabove, in some configurations, this may also be achieved by cooling therespective tissue area, for example via cryoablation.

In some configurations, energy such as RF energy may be delivered via asingle electrode, e.g., the electrode 103. In such configurations, theelectrical field can emanate away from the electrode as a single pointsource. In other configurations, energy may be delivered via a bipolarelectrode. In such configurations, and as described further herein, theelectrical field may emanate between two respective poles of theelectrodes (e.g., electrodes 103, 105). Such configurations may beadvantageous in facilitating adjustment of the treatment zone in thetissue region to be treated. Other configurations also are possible,including the use of multipolar electrodes or multiple separateelectrodes.

With reference now to FIG. 2, the catheter system 100 may be used fortreatment of tissue, for example pulmonary tissue. In some embodiments,the catheter system 100 is configured to be used in thoracoscopic,laparoscopic, transcutaneous, and/or percutaneous procedures. In somesuch embodiments, the catheter system 100 can be navigated to the noduleor other site of interest, within the body via fluoroscopy, tomographyor other external visualization techniques. In some configurations, thecatheter shaft 101 can be insertable into a bronchoscope 200. Varioustypes of bronchoscopes may be used, including but not limited to theBF-P180 bronchoscope manufactured by Olympus. Bronchoscopes usingultrasound probes or other visualization devices also can be used,including the EBUS® scope manufactured by Olympus (described in greaterdetail in FIG. 4 below). While the handle 120 is illustrated in FIG. 2at a distance from the bronchoscope 200 (and its working channel) forclarity, the handle 120 generally will be placed close to, or in contactwith, the working channel of the bronchoscope 200.

In some configurations, the catheter shaft 101 can be inserted into anairway 201 so that the distal end 109 of the catheter shaft 101 reachesor is placed proximate a region of tissue to be treated. For example,the catheter 101 can be inserted into the bronchoscope 200, which hasbeen inserted into the airway 201. Other configurations also arepossible. For example, when used relative to other body tissues and/orin other body lumens (e.g., during intestinal or colonoscopictreatments), the system 100 can be loaded into other types ofendoscopes. As will be described in greater detail below, the cathetersystem 100 can comprise a piercing component that is able to piercethrough an airway wall or lumen after the catheter shaft 101 is placedproximate a region of tissue to be treated, such as a lung nodule, forexample but without limitation. In other words, after the catheter shall101 passes along one or more airway of the lung, the piercing componentof the catheter system 100 can be used to pierce an airway wall or lumento gain access to tissue, nodules or the like outside of the airway. Insome configurations, the catheter system 100 can be passed through anairway and then extend into tissue outside of the airway while remainingwithin the pleurae. In some configurations, the catheter system 100enables piercing through the airway without contacting the chest wall.In some configurations, the catheter system 100 may be used without anendoscope, and may be used, for example but without limitation, intransthoracic or laparoscopic surgical interventions. In someconfigurations, it is contemplated that features may be added to thefirst electrode, the second electrode, or both to enhance visualizationwith x-ray fluoroscopy or ultrasound, for example. In someconfigurations, the surface area of the second electrode may be greaterthan the surface area of the first electrode. In some embodiments, asaline passage is provided along the internal surface of the firstelectrode. The surface area of the first electrode may be smaller thanthe surface area of the second electrode with the use of a fluid sourcedelivering saline or other fluids to the treatment area.

FIGS. 3A-3B illustrate the distal end 109 of the illustrated cathetershaft 101, which has been arranged and configured in accordance withcertain features, aspects and advantages of the present invention. Asillustrated, the distal end 109 may comprise one or more of the firstand second electrodes 103, 105. In some configurations, more than twoelectrodes can be positioned at or near the distal end 109. In someconfigurations, less than two electrodes can he positioned at or nearthe distal end 109. For example, one electrode can be positioned at ornear the distal end 109 and a patient pad can serve as the secondelectrode. Some configurations may provide for the first electrode 103being provided separately from the second electrode 105, or for three,four, or more electrodes being used to treat a region of tissue. Forexample, multiple catheters may be used to place the multiple electrodesinto contact with the tissue region to be treated.

In some configurations, the extreme distal portion of the distal end 109can provided with a piercing tip 310. The piercing tip 310 may be aseparate component from the electrode 103. In some configurations, thepiercing tip 310 can be a separate component from the electrode 103 butthe separate piercing tip 310 can be attached to the electrode 103. Insome configurations, the piercing tip 310 can be adhered to theelectrode 103. In some configurations, the piercing tip 310 can beformed integrally with the electrode 103 such that the piercing tip 310and the electrode 103 are monolithic and Unitary in construction. Thepiercing tip 310 can be formed, for example, by beveling or otherwisesharpening the distal end of the electrode 103.

The piercing tip 310 can be configured with a sharp edge 311 or end thatmay pierce, perforate, or penetrate into tissue, for example an airwaywall. In some configurations, the first electrode 103 can be positionedat the distal end 109, and even more preferably can be attached to,integrated to, or connected to the piercing tip 310. In other words, aportion of the first electrode 103 can be configured to comprising thepiercing tip 310 such that the first electrode 103 can pierce the airwaywall.

The second electrode 105 may be configured to be received in a movablemanner within or adjacent to the first electrode 103. In someconfigurations, the second electrode 105 can be extendible relative tothe first electrode and/or the first electrode 103 can be extendiblerelative to the second electrode 105. In some configurations, the handle120 may be used to move the second electrode 105 relative to the firstelectrode 103. Such a configuration will be described below withreference to FIGS. 6A-6C. In such a configuration, the second electrode105 may be movable along a longitudinal axis of the catheter shaft 101in, for example, a sliding manner.

Where the second electrode 105 is disposed within the first electrode103, only one electrode may need to be sufficiently strong to piercethrough an airway wall (e.g., with the piercing tip 310), rather thanneeding two separate electrodes possessing sufficient strength orrigidity or being provided with piercing tips arranged to puncture theairway wall. On the other hand, in some configurations, the secondelectrode 105 may be provided with, or attached to, a piercing end 312.The piercing end 312 can be used to penetrate into tissue being treated(e.g., a lung nodule). In some configurations, the piercing end 312 mabe sheathed by the first electrode 103. In some configurations, thepiercing end 312 may be exposed when the second electrode 105 isextended from the first electrode.

In some embodiments, the piercing end 312 may be flexible, butrelatively straight except for a slight curve at a distal tip thereof.When inserted into tissue, the piercing end 312 may curve or form aspiral or coil. In some configurations, the piercing end 312 can beformed or arranged to take a helical or spiral form. Such configurationsmay be preferable because they may induce an eddy current into thetissue being treated, in addition to the joule beating, resulting from aresistance of the tissue being treated. In some configurations, thepiercing end 312 is flexible, and adapts a helical, spiral, or coiledconfiguration once extended away from the first electrode 103. In someconfigurations, the piercing end 312 may comprise a superelasticmaterial (e.g., Nitinol) and the piercing end can change shapes. Othermaterials may also be used, including conductive polymers and bundles ofmultiple wires (such as a cable), which may in some configurationsprovide for greater elasticity.

As explained above, in some configurations, the piercing end 312 can bemanufactured at least in part from a shape-memory material, such asNitinol. In some such configurations, the piercing end 312 may have anaustenite configuration above body temperature that forms a coil orbend. The piercing end 312 may be loaded into the device 100 in themartensite configuration and in a straighter form, such that heating ofthe piercing end 312 (e.g., due to electric current passing through thepiercing end 312 or by contact of the piercing end 312 with warmer bodytissue) causes the piercing end 312 to convert to the austeniteconfiguration and form a bend or coil. In some configurations, thepiercing end 312 may be deployed into tissue while still straight,followed by subsequent heating, to cause it to change shape. In someconfigurations, the piercing end 312 may be heated as it is insertedinto the tissue (e.g., as it exits the electrode 103) so that it beginsto bend or coil as it is deployed. It is contemplated that deployment ofthe second electrode into a bent or coiled configuration may result inthe electrode assembly entering a tissue locking position such that thedistal tip of the device is maintained in position with respect to thetreatment area of interest. Such a locking position may be maintainedduring breathing or heat treatment. It is contemplated that the secondelectrode may go through multiple deployment from the first electrodewithout moving the first electrode. It is contemplated that the resultproduced from applying electrical energy to the device of the presentinvention may be an egg shaped ablation area instead of a sphere shapedablation area.

In some configurations, the outer dimensions of the coiled or helicalpiercing end 312 may be small enough to fit within the piercing end 310without bending. In some configurations, the piercing end 312 can beconfigured to embed or fixate itself into the surrounding tissue whenextended. For example, in some configurations, the piercing end 312 maycorkscrew or spiral into the surrounding tissue. Preferably, thepiercing end 312 may be shaped as a coil with a pitch in a range ofbetween about 0.1 mm to about 2 mm, and preferably about 1 mm. The majordiameter of the coil may measure between about 2 mm and about 10 mm, andpreferably between about 3 mm and about 4 mm. The coil may also comprisebetween about 0.5 total turns and about 5 total turns, and preferablybetween about 1,5 total turns and about 3 total turns. The wire diameterthat may be used to manufacture the coil may measure between about 0.010inches and about 0.020 inches, and preferably about 0.015 inches.

In some configurations, at least one of the first electrode 103 and thesecond electrode 105 includes an insulating layer 113, 115. In someconfigurations, for example, an insulating layer 113, 115 can bepositioned between the first electrode 103 and the second electrode 105.In some configurations, the insulating layer can be formed on an innersurface of the first electrode 103 and/or on an outer surface of thesecond electrode 105 (see, insulating layer 115 on the outer surface ofthe second electrode 105). Such a placement of the insulating layer(s)can serve to reduce the likelihood of short circuiting between theelectrodes while improving the use of bipolar or multipolar ablationconfigurations. In some configurations, the first electrode 103comprises an insulating layer 113 that terminates proximal of the distalextremity of the first electrode 103. In some such configurations, theinsulating layer 113 can be partially removed or stripped to expose oneor more conductive surfaces of the first electrode 103.

In some configurations, insulating materials may be lubricious.Lubricious insulating materials can improve the ability of theelectrodes 103, 105 to move relative to each other. Any suitableinsulating material may be used to overlay at least a portion of the oneor more electrodes. In some configurations, the insulating material maycomprise a polymeric material. For example, PTFE, fluorinated ethylenepropylene, high density polyethylene, polyethylene, and/or othersuitable insulating materials may be used. In some embodiments, the useof saline (e.g., saline conductive gel) can reduce friction between theelectrodes 103, 105. In some embodiments, one or more surfaces of theelectrodes 103, 105 can be coated with a ceramic powder.

When using bipolar or multipolar electrical ablation, in particular RFablation, the first and second electrodes 103, 105 can be used toconcentrate the energy being delivered to the surrounding tissue into azone roughly bounded by these electrodes 103, 105. The degree ofextension of the second electrode 105 into the tissue permits the userto modulate the amount and area of energy being directed into thesurrounding tissue. In some configurations, the first and secondelectrodes 103, 105 can be configured to limit the range of relativeextension. For example, the range of relative extension between thefirst and second electrodes 103, 105 can be predetermined based upon thesize of the nodule or other area of interest to be treated. In someembodiments, the deployed distance between the first and secondelectrodes 103, 105 is configured to be approximately equal to the depthof the nodule or other area of interest into which the first and/orsecond electrodes 103, 105 are deployed. In some configuration, theextent to which the first and second electrodes 103, 105 can moverelative to each other in the distal and/or proximal directions isapproximately equal to the distance required to move the proximal end ofthe second electrode 105 from the stored position to the deployedposition. In some embodiments, the extent to which the first and secondelectrodes 103, 105 can move relative to each other in the distal and/orproximal directions is greater than the deployed distance between thefirst and second electrodes 103, 105 due, for example, to the secondelectrode 105 being stored in a relative straight configuration withinthe catheter shaft 101 prior to deployment.

As illustrated in FIG. 3, the second electrode 105 can be configured toextend from the first electrode at an angle A1 from the centerline CL ofthe first electrode 103. In some embodiments, the angle A1 at which thesecond electrode 105 is extended can be greater than or equal to about0° and/or less than or equal to about 180°. In some embodiments, theangle A1 is approximately 90°. Many variations are possible. Forexample, FIG. 3D illustrates an embodiment wherein the angle A1 at whichthe second electrode 105 extends from the first electrode 103 isapproximately equal to 180°. In some embodiments, the second electrode105 is configured to wrap around the first electrode 103 and/or distalend 109 of the catheter shaft 101.

In some embodiments, the distal end 109 of the catheter shaft 101 caninclude one or more apertures 111. The second electrode 105 can beconfigured to extend through the aperture 111 when transitioned to thedeployed position. In some such embodiments, the second electrode 105can extend to a position proximal to, lateral to (e.g., the secondelectrode 105 can extend at an angle A1 from the centerline CL of thefirst electrode 103), and/or distal to the first electrode 103.

As illustrated in FIG. 3F, the second electrode 105 can be fixed to theexterior surface of the distal end 109 of the catheter shaft 101. Forexample, the second electrode 105 can be fixed to one or more conductivecontact points 113, 114 configured to electrically connect the secondelectrode 105 to one or more of the first and second electrical leads107, 108. In some embodiments, an externally-affixed second electrode105 can be configured to function as an auger threading to permit thedistal end 109 of the catheter shaft 101 to advance into tissue as thedistal end 109 of the catheter shaft 101 is rotated (e.g., in rotationdirection DR, as illustrated in FIG. 3F). The second electrode 105 canreduce or eliminate the likelihood of the electrodes 103, 105 detachingfrom the tissue into which the are inserted absent rotation of thedistal end 109 of the catheter shaft 101 in a direction opposite therotation direction DR.

In some embodiments, the piercing tip 310 of the first electrode 103 isused to pierce the wall 3 of an airway 1. The first electrode 103 and/ordistal end 109 of the catheter shaft 101 can include a slot 111 a. Theslot 111 a can extend through a side wall of the first electrode 103from the distal end of the first electrode 103 to a point proximal tothe distal end of the first electrode 103. The second electrode 105 canbe configured to extend through the slot 111 a at an angle A2 from thecenterline of the first electrode 103 as the second electrode 105deploys from the first electrode 103. The angle A2 can be greater thanor equal to about 0° and/or less than or equal to about 180°. In someembodiments, the angle A2 is approximately 90°.

During deployment, the first electrode 103 can be advanced through anairway wall 3 tangentially to a nodule 208 or other site of interestoutside of the airway 1. The second electrode 105 can be advanced atangle A2 from the first electrode 103 into the nodule 208. The piercingend 312 of the second electrode 105 can pierce the nodule 208. Thepiercing end 312 can, in some embodiments, include a barb or otherfixation feature to reduce or eliminate the likelihood, that thepiercing member 312 disengages from the nodule 208. Upon deployment ofthe second electrode 105, the first electrode 103 can continue toadvance in the distal direction F. Further advancement of the firstelectrode 103 can increase the angle A2 between the centerline of thefirst electrode 103. In some embodiments, first electrode 103 cancontinue to advance in direction F such that the second electrode 105 ispositioned proximal to the first electrode 103. In some embodiments, aninsulating layer 113 on the first electrode 103 can help to reduce oreliminate the likelihood of damage to the airway wall 3 from electriccurrent introduced to the first electrode 103.

Piercing through the airway wall or lumen in some of the embodimentsdescribed above may present some advantages in the treatment of lungtissue and nodules. Such transluminal approaches permit the energydelivery to be approximately centered into the mass to be treated,compared to intraluminal approaches that may remain the airway. At thesame time, transluminal approaches are less invasive and may he able toaccess deeper sections of the lung with less trauma and complicationsthan conventional transthoracic approaches.

In some embodiments, all or a portion of the one or more of theelectrodes 103, 105 may be detachable and/or interchangeable with otherelectrodes. For example, the piercing up 310 or the piercing end 312 maybe configured to detach from the remainder of the respective electrodeto which it is attached to. In some embodiments, the catheter system 100can be sold with multiple piercing tips 310, piercing ends 312, firstelectrodes 103, and/or second electrodes 105 (hereinafter referredcollectively as detachable components). Each of the detachablecomponents can be sized and shaped to treat a particular range of nodulesizes (e.g., width/volume) and/or to accommodate particular ranges ofpower requirements or fluid uses for the treatment of a particularnodule or other area of interest. In some embodiments, the appropriatedetachable components can be chosen after visualizing the area ofinterest (e.g., nodule, tumor, and/or lesion) and/or after biopsyingtissue from the area of interest. When detached while embedded intissue, the detached section may be used as a fiducial marker or otherindicator suitable to indicate the location of the area that wastreated. This may be useful not only in post-treatment diagnoses, butalso in serving as a navigational aid for subsequent treatment.

Because the lungs generally have airway sizes of decreasing diameter andincreased convolution, treatment modalities may need to be varied inresponse to the pulmonary area being treated. The central lung,extending from the trachea to the larger (i.e., left and right) mainbronchi, and the mid-lung region, which may comprise lobar and segmentalbronchi, are typically large enough to be navigated with a bronchoscope.Accordingly, treatment of affected areas in the lung, which may includelung nodules and other such diseased regions, may be performed withrelative ease in the central lung. Treatment into mid-lung region, whilemore difficult, can be performed using bronchoscope-based treatmentmethods. In particular, bronchoscopes with side-facing ultrasound probes(such as the Olympus EBUS® scope) may be particularly well suited fortreatment of regions of lung tissue such as lung nodules, especiallythose located on an opposite side of an airway wail that a bronchoscopeis located on. Access to highly angulated lung regions may still bedifficult in some situations.

Peripheral regions of the lung, however, comprise subsegmental bronchileading to terminal bronchi and alveoli, and may be too small or toohighly angulated to be navigated with traditional visualization means.Navigating to and treating such peripheral regions may thus require abronchoscope or other guide means to be inserted as far as possible,followed by extension of a much smaller guide sheath into the peripheralregions. Guidance to the peripheral region in such cases may be providedusing fluoroscopy or other non-bronchoscopic visualization methods.These methods may also be useful in larger airways that are highlyangulated and thus difficult or impossible to reach via bronchoscopicapproaches.

Bronchoscopes or other endoscopes provided with ultrasound probes orotherwise used in conjunction with ultrasound may also be used inconjunction with Doppler or other blood flow visualization means.Especially in a highly-vascularized environment such as the lung,visualization of blood flow may be advantageous to avoid causingexcessive bleeding or delivering large amounts of energy to bloodvessels.

FIG. 4 illustrates an embodiment of the catheter system 100 disposedwithin a bronchoscope 500 provided with a side-facing ultrasound probe502 placed within an airway 201. An example of such a bronchoscope 500is the EBUS® scope manufactured by Olympus. Preferably, the bronchoscope500 is provided with at least one lateral port 504 extending from thebronchoscope working channel; this permits the catheter shaft 101 toextend through the port 504.

In some configurations, the first electrode 103, being preferablyprovided with a piercing tip 310, is bendable and flexible. In someconfigurations, the first electrode 103 and/or the piercing tip 310 maybe bendable at an angle of at least 10°, preferably about 20°, about30°, about 45°, about 55°, about 65°, about 75°, and even morepreferably at least about 90°, relative to the longitudinal axis of theaxial length of the airway. As such, when a region of lung tissue to betreated is located—for example, by use of the side-facing ultrasoundprobe 502—the first electrode 103 can be extended at least partiallyinto that region of lung tissue by piercing through the airway 201. Thefirst electrode 103 and/or piercing tip 310 may not necessarily need tobe bendable, and can be used, for example, to pierce a tissue sitedisposed directly in front of the catheter system 100. In someconfigurations, the second electrode 105 and/or its piercing end 312 canbe configured to extend from within the electrode 103 into the lungtissue distal of the airway wall. Some examples of flexible needles thatmay be used in conjunction with embodiments disclosed herein may befound in U.S. Application Ser. No. 61/604457, filed Feb. 28, 2012,titled “LUNG BIOPSY NEEDLE,” and U.S. application Ser. No. 13/777,854,filed on Feb. 26, 2013, titled “LUNG BIOPSY NEEDLE,” both of which arehereby incorporated by reference herein in their entirety.

In some cases, however, and as discussed above, regions of lung tissueto be treated may be found in peripheral lung regions. In peripherallung regions, the air passages are too small to be navigated withconventional bronchoscopes, and much smaller instrumentation must beused to navigate treatment methods and devices to regions of tissuewithin this region. Typically, a small diameter bronchoscope isnavigated as deeply as possible in the lung, at which point a guidesheath may be extended to reach the peripheral tissue to be treated.Embodiments of the catheter system 100 may thus be miniaturized to fitinto small bronchoscopes, for example those with a working channelhaving a 3 mm outer dimension and a 2 mm working channel. Guide sheathsmay have an outer diameter of about 1.95 mm and a somewhat smaller innerchannel, and the catheter system 100 and the sheath 101 may beconfigured to pass within these channels. Although some embodiments maynot be able to reach into the smallest individual alveoli, these may beable to reach deeply enough into the lung so as to be positioned in anairway proximate a region to be treated.

In some configurations of the catheter system 100 configured to beguided to positions within the peripheral lung regions 203, the cathetersystem 100 (which may still be disposed within a guide sheath) may beguided using external guidance methods. For example, guidance may beeffectuated via real time computerized tomography (“CT”), viaelectromagnetic navigation (e.g., the SuperDimension iLogic system), viavarious transthoracic tools, or via fluoroscopy.

FIG. 5 illustrates a cutaway view of an embodiment of the handle 120.Here, the handle 120 comprises a second activation toggle 122 that ispreferably configured to extend the second electrode 105, wherein theproximal end of the second electrode 105 is attached within the secondactivation toggle 122 (for example, within a cavity). The secondactivation toggle 122 may be connected in a movable manner via one ormore movable rods 128 to the first toggle 124. The first toggle 124 maybe configured to extend the first electrode 103. Details of these stepswill be described in FIGS. 6A-C.

In some configurations, a first hypotube 129 extends through a centralpassage of the first activation toggle 124 and into a handle base 126and the second activation toggle 122. The first hypotube 129 can befixedly attached within the first activation toggle 124, but remains ina movable (e.g., slidable) relationship with the handle base 126 and thesecond activation toggle 122. The first hypotube 129 also extends withina second hypotube 130 that is disposed in a movable manner (e.g., in asliding manner) between the handle base 126 and the first activationtoggle 124. The second hypotube 130 can be fixedly attached within thehandle base 126, and can slide in relation to the first activationtoggle 124.

The electrical lead 108 can be configured to be electrically connectedthrough an aperture in the second activation toggle 122 to the secondelectrode 105. In some embodiments, a proximal portion of the secondelectrode 105 may extend along the entire length of the first hypotube129 and be fixedly secured within a cavity in the second activationtoggle 122. The electrical lead 108 may be connected to the secondelectrode 105 via a cable or other electrical connector, and may in someembodiments extend, when provided with suitable insulation, along all orpart of the first hypotube 129. Preferably, the second electrode 105and/or electrical lead 108 are insulated along their entire length, andparticularly in relation to the catheter shaft 101.

In some configurations, the proximal end 110 of the catheter shaft 101extends through the handle base 126 and the first activation toggle 124,and is received in a movable manner within the second activation toggle122. The proximal end 110 can be fixedly attached within the handle base126, for example via a bushing 134 (which may be placed entirely orpartly within the second hypotube 130).

In some embodiments, the handle 120, and in some configurations thesecond activation toggle 122 of the handle 120, comprises one or morestops configured to reduce or eliminate the likelihood of variouscomponents, such as the first and second activation toggles 122, 124,from being overextended or detached. For example, the first hypotube 129may comprise a stop with a nub or other projection that is configured toreduce or eliminate the likelihood of the hypotube being overextended.Such stops may also or alternatively be placed on the movable rods 128.

The first activation toggle 124 can have the electrical lead 107connectable thereto. The electrical lead 107 can be configured to beelectrically connected to the catheter shaft 101, for example through aconductive hypotube 129, both of which can be electrically conductive soas to transmit electricity to the first electrode 103. In otherembodiments, the electrical lead 107 is configured to be electricallyconnected via the aperture to the first electrode 103 via a separatecable or wire.

FIGS. 6A-C illustrate different deployment stages of the system 100. ingeneral, embodiments of the catheter system 100 may be configured with ahandle portion 120 that permits the electrodes to be engaged ordisengaged (for example, extended or retracted) with relative ease by anoperator. An example of such a system is illustrated here. For example,the handle 120 may be configured to have one or more activation toggles(e.g., as described above in FIG. 5) that permit the first electrode 103to be extended from the catheter shaft 101 and/or the end of abronchoscope or other such instrument that the catheter system 100 maybe inserted into FIG. 6A, illustrates the handle 120 in a state wherethe first electrode 103 is retracted within a working channel of abronchoscope or guide sheath (not illustrated).

Turning now to FIG. 6B, the first activation toggle 124 has been moveddistally toward the handle base 126. Preferably, the first activationtoggle 124 is slid along the second hypotube 130, but other movementmodes are envisioned, such as having a screwable or rotationalengagement. This movement of the first activation toggle 124 may pushthe first electrode 103 out of the catheter shaft 101. In someconfigurations, the electrode 103 can be integral with the cathetershaft 101 and movement of the first activation toggle 124 may serve toadvance the catheter shaft 101 and the first electrode 103 by a smalldistance, for example a distance sufficient to permit the electrode 103to extend out of a bronchoscope working channel and/or guide sheath. Inany event, when provided with a piercing tip 310, these arrangements mayenable the first electrode 103 to pierce into and be placed into atissue site. This may include, for example, piercing through an airwaywall.

In FIG. 6C, with the first activation toggle 124 displaced, the secondactivation toggle 122 may then be moved distally in the direction of thefirst activation toggle 124. Preferably, the second activation toggle122 is slid along the one or more slider rods 128 and/or the firsthypotube 129. As mentioned above, alternate movement mechanisms areenvisioned, including screwable or rotational engagements. The movementof the second activation toggle 122 permits the movement of the secondelectrode 105, thereby allowing the second electrode 105 to slide andextend from the first electrode 103. Preferably, this longitudinalmovement embeds or fixes the second electrode 105 into the tissue to betreated. It will be noted that in some embodiments, all or part of theforegoing toggle mechanisms that permit engagement of the one or moreelectrodes may be motorized.

FIG. 7 illustrates a cutaway view of the first activation toggle 124. Insome configurations, it may be desired to include a fluid port 830 influid communication with one or more of the electrodes 103, 105 and/orthe tissue region to be treated. In some configurations, the fluid port830 can be in fluid communication with the catheter shaft 101, and canthereby be connected to a source of fluid (described in greater detailbelow). For example, an aperture may be made into the first hypotube 129such that fluid introduced through the fluid port 830 enters into thehypotube 129 and flows proximally toward the central cavity in thesecond activation toggle 122. The fluid may then flow down the hollowcatheter shall 101. In some configurations, appropriate seals andinsulation can be provided to improve the mechanical and electricalintegrity of the device.

In some configurations, the fluid port 830 may he disposed in the secondactivation toggle 122, or elsewhere on the device. In someconfigurations, the fluid port may communicate to a dedicated fluidchannel that runs along or through the catheter shaft and/or electrodes.The location of the fluid port 830 may not necessarily be on the firstactivation toggle 124, and may instead be mounted on any other portionof the handle 120, or provided separately onto the catheter shaft 101.

FIGS. 8A-D illustrate a variation of the embodiment described above inrelation to FIGS. 6 and 7A-C. With reference now to FIG. 8A, anembodiment of a handle 120 that may be used with the system 100comprises a handle base 126 that is connected in a movable manner to afirst activation toggle 124 via a second hypotube 130. At the proximalend of the handle 120, a second activation toggle 122 is attached via afirst hypotube 129 and/or catheter shaft 101. Although there are somesimilarities in the general functionality of this embodiment incomparison to the embodiment discussed previously, there are severalchanges and additional parts.

The handle 120 may comprise a bronchoscope attachment 140, optionallyprovided with a bronchoscope guide 142 attached at its distal end andextending in a distal direction. This attachment 140 is preferablyconfigured to be secured to the exterior of the working channel of abronchoscope, with the bronchoscope guide 142 being preferably extendingat least partly into the working channel. Such an arrangement, whileoptional, may aid the operator in controlling and handling the cathetersystem 101.

Although some embodiments may provide for the bronchoscope attachment140 to be integrated into or permanently attached to the handle base126, the embodiment described provides for a removable bronchoscopeattachment 140. Such an arrangement may permit different bronchoscopeattachments to be supplied for use with different bronchoscope orendoscope types. In a preferred embodiment, the bronchoscope attachment140 is secured to the handle base 126 by using a second thumb grip 141attached to the handle base 126. The second thumb grip 141 can bereceived into a slot 143 and turned so as to tighten the second thumbgrip 141 against the bronchoscope attachment 140, in some configurationsafter the attachment 140 and guide 142 have been set to the correctdepth within the bronchoscope working channel. Other attachmentmechanisms are contemplated, including various latches, screwingengagements, and the like.

As with the embodiment previously described, the thumb grip 121 may beprovided to aid an operator in manipulating and controlling the cathetersystem 101. In some embodiments, the thumb grip 121 may also be used tolock the piercing end 310 of the first electrode 103 after it has beeninserted into tissue, using deployment steps such as those describedbelow, for example but without limitation. In some configurations, thesecond activation toggle 122 can be configured to be connected to theremainder of the handle 120 via the first hypotube 129 and/or thecatheter shaft 101. These respective parts being generally flexible, thesecond activation toggle 122 can be deployed from any angle. A furtheradvantage is that in some embodiments, as illustrated, the toggle 122may be more ergonomic and easily grasped compared to other embodiments.

FIGS. 8B-D illustrate cutaway views of the embodiment discussed above inrelation to FIG. 8A. In this embodiment, the second activation toggle122 comprises a static grip 152, which preferably comprises a centralcavity into which the proximal end of the second electrode 105 may bereceived. The proximal end of the second electrode 105 can be attachedto a holder 154. The holder 154 may then be secured or attached to thestatic grip 152. In some embodiments, an ergonomic knob 158 may beprovided at a distal end of the static grip 152. The ergonomic knob 158may be C-shaped, or otherwise adapted to be grasped by a thumb or fingerof an operator.

A movable grip 156 can be disposed around the static grip 152, and canbe movable in relation to it. In some configurations, the movable grip156 can be movable in a longitudinal axial direction with respect to thestatic grip 152. As such, moving the movable grip 156 in a proximaldirection (i.e., toward the ergonomic knob 158) will act to move theelectrode 105 in a distal direction, thereby deploying it from thedistal end of the catheter shaft 101. In some embodiments, the cathetershaft 101 and/or first hypotube 129 may be attached or in a frictionalengagement with the movable grip 156, so as to permit the secondelectrode 105 to be longitudinally axially displaced in relation tothese.

In some configurations, an opposite engagement can be used in which theholder 154 is attached to the movable grip 156, such that moving, themovable grip 156 in a distal direction (i.e., away from the ergonomicknob 158) will deploy the second electrode 105. In this embodiment, thecatheter shall 101 and/or first hypotube 129 may remain attached or infrictional engagement with the static grip 152. Other engagements arealso possible. In some embodiments, the second activation toggle 122 (orany other part of the handle 120) may also be provided with a lock orother means to prevent accidental deployment of the catheter system 101.Additionally, it will be recognized that electrical leads 107 and 108,may be disposed on the first and second activation toggles 124, 122, orelsewhere on the handle 120. In some configurations, the firstelectrical lead 107 (connected or connectable to the first electrode103) is attached to the first activation toggle 124. In someconfigurations, the second electrical lead 108 (connected or connectableto the second electrode 105) is attached to the second activation toggle122, for example on the movable grip 156 via a bolt or other solidattachment. Further, a fluid entry port 830 may also be present on thefirst activation toggle 124 or elsewhere on the handle 120 in a mannersimilar to what has been previously described. For example, the fluidentry port 830 can be located on the first activation toggle 122.

With reference now to the distal end of the handle 120 illustrated inFIG. 8C, the relationship between various components comprising theillustrated catheter system 100 can be clarified. As illustrated, thebronchoscope guide 142 can be attached to the bronchoscope attachment140. The guide 142 can be constructed from a lubricious and flexiblematerial, including polymers, such as polyurethane,polytetrafluoroethylene, high density polyethylene, PEEK, polyamide, andthe like. The bronchoscope guide 142 (together with the bronchoscopeattachment 140) may be helpful in allowing an operator to position thecatheter shaft 101 and other components of the system 100 into abronchoscope working channel.

A guide sheath 145 is optionally disposed on an outer surface of thecatheter shaft 101, and can extend distally past the distal end of thebronchoscope guide 142 and proximally into the handle base 126. It maybe secured therein, for example by using the second thumb grip 141. Theguide sheath 145 can be constructed from a flexible and lubriciousmaterial (including polymers such as polyurethane andpolytetrafluoroethylene), and can be preferably at least partly abrasionresistant. As such, the guide sheath 145 can be used to protect thedistal end 109 of the catheter shaft 101, such as the piercing ends 310,312. Further, the guide sheath 145 can be sized to extend at least theentire length of the bronchoscope working channel. Consequently, theguide sheath 145 can also be used to protect the bronchoscope workingchannel from abrasions or other damage resulting from the catheter shall101. The catheter shaft 101 can have the second electrode 105 disposedthere within.

In some embodiments, the guide sheath 145 may be extended far past thebronchoscope working channel so as to reach deep lung regions or lungregions that are too narrow or angled to be reachable by a traditionalbronchoscope. In such cases, the guide sheath 145 may be guidedfluoroscopically or using other navigational methods to a region oftissue to be treated. Consequently, some embodiments may be providedwith a localization marker such as a radioopaque marker disposed at theend of the guide sheath so as to aid in navigation.

Turning now to FIG. 8D, an enlargement of an embodiment of the secondactivation toggle 122 is illustrated. The catheter shaft 101 can extendall the way to the second activation toggle 122, and may be attached orin frictional engagement with the static grip 152 or the movable grip156. In some configurations, the second electrode 105 is disposed withinthe catheter shaft 101 and extends into and is attached to the holder154. In some COD figurations, the first hypotube 129 may be provided.Instead of being disposed on the outside of the catheter shaft as in theconfiguration illustrated in FIG. 5, the first hypotube 129 can bedisposed on the interior of the catheter shaft 101, and over theproximal end of the second electrode 105. As such, the hypotube 129 maybe useful to provide additional rigidity and structural support to thesecond electrode 105. Further, the hypotube 129 may be useful inmaintaining fluid introduced via a fluid port 830 within the cathetershaft 101.

FIG. 8E illustrates another embodiment of a catheter system 100′.Numerical reference to components is the same as previously described,except that a prime symbol (′) has been added to the reference. Wheresuch references occur, it is to be understood that the components arethe same or substantially similar to previously-described components.For example, the catheter system 100′ includes a first activation toggle124′ that has an elongated body. The catheter system 100′ can includehandle 120′. The handle 120′ can include a thumb pad 121′ shapedgenerally as a collar with a protrusion extending from the handle 120′.In some embodiments, the catheter system 100′ includes a bronchoscopeattachment 140′ configured to slidable engage an interior of a handlebase 126.

FIG. 9 illustrates the distal end 109 of the catheter shaft 101. Asillustrated, a fluid source has been connected to the catheter shaft 101for example via the fluid port 830), and fluid 901 is shown exiting thespace between the first electrode 103 and the second electrode 105. Inthis manner, fluid 901 can be injected proximate the respectiveelectrodes 103, 105 when the electrodes are deployed in a region oftissue to be treated. Of course, other configurations are possible, andin sortie configurations the fluid source does not leave the cathetershaft 101, and may be sealed within all or part of the system 101, forexample in a recirculating arrangement. In some configurations, thefluid 901 may circulate within one or both of the first and secondelectrodes 103, 105. Also, other configurations may permit the fluid 901to be dispensed or injected from other regions, including, aperturesproximal to the electrodes 103, 105 along the catheter shaft 101, forexample. In some configurations, one or both of the first and secondelectrodes 103, 105 may be hollow and at least partially porous (i.e.,using a sintered manufacturing method) or provided with one or moresmall holes, thereby permitting the fluid 901 to be dispensed therefrom.

The fluid 901 may be used for several purposes. In one embodiment, thefluid 901 acts to cool the electrodes 103, 105. In general, whenelectrodes are heated, for example when delivering RF energy, electrodeefficiency may be reduced due to increased impedance. As a result,cooling the electrodes may be beneficial to maintaining electrodeperformance during energy application to tissue. While the fluid 901 maybe a liquid, in some embodiments it may be a gel or other flowablesubstance.

The fluid 901 may also be beneficial in reducing or eliminating thelikelihood of tissue charring when delivering energy to beat the tissue.In particular, for RF ablation and other electrically-based heatingtechniques, if tissue is heated at too high of a temperature, the tissueis likely burn or char. Once this occurs, the impedance of the tissueincreases, thereby reducing or eliminating the likelihood of theablation treatment reaching a larger area of tissue due to the greatlyreduced tissue conductivity. Therefore, a larger tissue region can betreated with heat as long as the tissue is maintained at a temperaturebelow which the tissue burns or chars. The fluid 901 may be useful forpromoting this result.

Additionally, in embodiments where the fluid 901 is injected into tissuesurrounding the electrodes 103, 105, the fluid 901 may be beneficial inconducting heat to a larger area of tissue. This may enable a largerarea of tissue to be treated than if no fluid were injected. In RFablation in particular, care must be taken to not significantly overheator “char” the tissue surrounding the electrodes while heating the tissuesufficiently to denature, deactivate, or kill the targeted tissue. Byinjecting fluid 901 in the vicinity of the tissue surrounding theelectrodes, heat may therefore be spread to a wider area.

In some embodiments, the fluid 901 comprises a saline solution. In someembodiments, the solution may comprise between about 0.1% to about 34%saline, more preferably about 0.7 to about 1% saline, and even morepreferably about 0.9% saline. Other solutions containing electrolytesare possible, including phosphate buffer saline (PBS) and the like. Thefluid 901 may in some embodiments also comprise a conductive gel. Whenusing a saline or otherwise electrolytic solution in a fluid 901 that isinjected into the tissue surrounding the electrodes, tissue conductivitymay be increased. As described above, this may increase the dimensionsof the area treatable with the electrodes. In particular, for methodsthat heat tissue with electrical energy (e.g., RF ablation), suchheating may dry tissue, thereby reducing its conductivity. The additionof an electrolytic solution may thereby also help mitigate any sucheffect. In some embodiments, it has been found that a saline infusionrate preferably between about 1 and about 10 ml/min, more preferablyabout 2-6 ml/min, functions well as a balance between increasing thetreated area while reducing, or eliminating the likelihood of injectingof large volumes of fluid into the tissue (which may open up a voidspace or fluid pocket which may be undesirable in some treatmentmodalities).

Because lung tissue is less dense than tissue in other body organs andregions (e.g., the liver), such lung tissue may have a higher impedancethat can hamper efforts to deliver energy sufficient to treat or ablatetissue. As such, dispensing a saline solution may be more advantageousin pulmonary tissue compared to other, denser types of tissue.Particularly, but not exclusively, when coupled with embodiments usingtransluminal piercing electrodes that extend through an airway wall(rather than being disposed in contact with the airway wall), this maypermit treatment of lower-density tissue surrounding a higher-densitymass such as a lung nodule. This may also be advantageous in thetreatment of lower-density nodules, such as ground-glass opacitynodules.

In any event, the ability to treat tissue with higher impedance may beespecially useful when treating lung nodule margins. Whereasconventional ablation or energy delivery treatment techniques may not beable to account for differences in tissue impedance between higherdensity nodules and lower density tissue surrounding the nodules, it isbelieved that use of at least saline or electrolytic fluid may beadvantageous in treating margins around tissue by reducing the impedanceof the lower density tissue. For example, as lung nodule with anapproximate diameter of less than 3 cm may have margins removed aroundit that are at least 2 cm in size. Accordingly, treatment of thelower-density tissue margins surrounding a higher density nodule may beperformed in a single step through the infusion of fluid.

In some embodiments, the fluid 901 may comprise additional agents, Forexample, medicants, such as antimicrobial, antiviral, anticancer,anti-tumor, anti-inflammatory, pro-inflammatory, and other suchcompounds or substances may be introduced. Cells, including stem cells,as well as cell growth promoters or inhibitors may also be used. Thefluid 901 or a component thereof may also coagulate, solidify, or act asa sclerosing agent, for example after being heated, cooled, or activated(e.g., via a polymerization initiator). Such a fluid may be useful if asvoid is created as a result of fluid delivery, or so as to encapsulatethe tissue region being treated. Examples of such fluids 901 compriseheat curing epoxies, thermoset resins (e.g., polyurethane, polyester),and protein complexes (e.g., egg whites).

Further, the fluid 901 may also comprise visualization agents. Theseagents may be beneficial in indicating the extent to which the fluid 901has spread within the tissue being treated, and could be used todemarcate an approximate treatment area. In some embodiments, thevisualization agents may comprise pigmented or colored substances. Thevisualization agents may also be at least partially radioopaque, or actas MRI-contrast enhancing agents. In some embodiments, the visualizationagent may include antibodies or other indicators capable of binding to aparticular tissue type (e.g., cellular cancer markers) so as to permitvisualization of an affected region of tissue.

The catheter system 101 may also comprise additional sensors. Thesesensors are preferably configured to monitor one or more attributes ofthe system 101 and/or its effect on the tissue being treated. Anon-limiting example of some monitored attributes that may be monitoredinclude temperature monitoring (including for example monitoring of thetreatment site, of the fluid, and/or of the electrodes), monitoring ofelectrical parameters associated with the electrodes (including forexample impedance, voltage, and/or current), and monitoring of the fluidflow rate and amount thereof dispensed. When monitoring temperature,some embodiments may be configured to have one or more temperaturesensors able to detect the temperature of the surrounding tissue. Thistemperature sensor may be attached or integrated with one or more of thefirst and second electrodes 103, 105, or in some embodiments may beprovided as a separate temperature probe.

In some embodiments, an impedance sensor may be useful to monitor theimpedance of either or both of the electrodes and tissue being treated,and may be integrated into the electrodes or present as a separatesensor. Impedance may be a useful measurement to determine whether theelectrodes are being overheated, whether the tissue being treated isdehydrated, and/or whether the tissue is being overheated, which mayresult in the tissue charring or burning. As previously noted, charredor burned tissue will have a markedly higher impedance, whichconsequently requires greater power to ablate, but also limits theextent to which energy can be dispersed into the surrounding tissue.

The catheter system 100 may be provided with a feedback mechanismconfigured to change one or more treatment attributes based uponmonitored attributes received from one or more sensors, including thesensors described above, or time. The feedback mechanism may be used tochange treatment attributes including the amount and type of power beingapplied to the tissue, the frequency of the power applied, the flow rateof the fluid, and other such attributes.

In one embodiment, the feedback mechanism may stop or decrease theapplication of power via the electrodes if the tissue or electrodetemperature or impedance increases at too high of a rate or beyond apredetermined limit. Additionally, the feedback mechanism may be used totrigger one or more predefined treatment modes, although such predefinedtreatment modes may not necessarily need to be triggered by the feedbackmechanism or any monitored attribute in particular, and may be usedindependently of such (for example, after passage of a certain timeperiod rather than in response to one more monitored attributes ortreatment attributes). A predefined treatment mode, may, for example,include time intervals where application of power is modulated or madeintermittently active. A feedback mechanism may, for example, be used tomodulate the power applied based on the temperature, and could lower thepower applied during a predetermined time interval when the tissuereaches a certain temperature, and raise the power applied after thattime interval if the tissue temperature has decreased. The timeintervals and other predefined treatment modes may also be determinedalgorithmically based on real-time monitoring of the tissue and/orelectrodes, and are not necessarily determined or defined prior tobeginning of the treatment.

FIG. 10 illustrates additional electrode assembly configurations thatmay be used in some embodiments of the catheter system 100. Electrodeassembly 1201 is an expanding “basket” type electrode with a firstproximal electrode 1203 and a second distal electrode 1205, separated byan insulator portion 1204. An additional insulator portion 1206 may alsobe present proximal of the first electrode 1203. When deployed andpushed against or into tissue, the multiple strands that make up the“basket” of the second electrode 1205 push apart, thereby expanding theregion that may be treated with electrical energy.

Electrode assembly 1211 illustrates an embodiment of a multi-wirepenetrating, electrode. Here, the first proximal electrode 1213 isseparated from the multi-wire second electrode 1215 by an insulatorportion 1214. When deployed or pushed against or into tissue, theindividual wires of the second electrode 1215 penetrate into tissue,thereby increasing the zone that may be treated with electrical energy.Additionally, the individual wires of the second electrode 1215 may alsoserve to fixate the electrode 1215 into the tissue being treated.

Electrode assembly 1221 illustrates an embodiment of an electrode with astraight coil, similar to the electrode design illustrated in FIGS.3A-B, but where a second distal electrode 1225 will not retract into afirst electrode 1223. The electrodes are separated from each other by aninsulating portion 1224.

Electrode assembly 1231 illustrates an embodiment of an electrode with afirst electrode 1233 and a spherical coiled second electrode 1235. Therespective electrodes are separated from each other by an insulatingsection 1234.

Of course, it will be clear that the above electrode types, as well asthe other electrodes described herein, are non-limiting embodiments, andthat other electrode types are possible. In terms of electrode design,in some embodiments it may be preferable to increase the total surfacearea of the electrode, in particular the second electrode or anelectrode which extends into tissue. Electrodes comprising additionalfingers or prongs may thus be desirable. Further, some embodiments maycomprise one or more electrodes that are roughened or textured, or whichmay have nanoparticles embedded or sintered thereto, or other nanometeror micrometer size features deposited, etched, or machined thereupon. Anotch or other channel may also be provided on some embodiments ofelectrodes described herein, and may be used to aid in delivering fluid901 to the tissue being treated.

Although this invention has been disclosed in the context of certainembodiments and examples, those skilled in the art will understand thatthe present invention extends beyond the specifically disclosedembodiments to other alternative embodiments and/or uses of theinvention and obvious modifications and equivalents thereof. Inaddition, while several variations of the invention have been shown anddescribed in detail, other modifications, which are within the scope ofthis invention, will be readily apparent to those of skill in the artbased upon this disclosure. It is also contemplated that variouscombinations or sub-combinations of the specific features and aspects ofthe embodiments may be made and still fall within the scope of theinvention. It should be understood that various features and aspects ofthe disclosed embodiments can be combined with, or substituted for, oneanother in order to form varying modes or embodiments of the disclosedinvention. Thus, it is intended that the scope of the present inventionherein disclosed should not be limited by the particular disclosedembodiments described above.

What is claimed is:
 1. A device for the delivery of energy to a regionof lung tissue, the device comprising: a guide sheath; a catheterconfigured to be inserted into the guide sheath; a first electrodeattached to the distal end of the catheter, wherein the first electrodeand the catheter are hollow, thereby forming a channel enclosed by thefirst electrode and the catheter, wherein the first electrode comprisesa piercing tip configured to pierce through an airway wall; a secondelectrode received in a movable manner within the channel of the firstelectrode, wherein the second electrode is in a first configuration whenwithin the first electrode, wherein when a distal end of the secondelectrode extends distally from the first electrode, a portion of thesecond electrode that is extended from the first electrode changes fromthe first configuration to a second configuration; a first electricallead in electric communication with the first electrode; and a secondelectrical lead in electric communication with the second electrode,wherein the first and second electrical leads are connectable to asource of electric power, wherein the second configuration comprises ahelical configuration, wherein in the first configuration the secondelectrode conforms to the channel of the first electrode, wherein thefirst configuration is not a helical configuration.
 2. The device ofclaim 1, further comprising a handle attached at a proximal end of thecatheter, wherein the handle comprises an activation toggle configuredto extend the second electrode from the first electrode.
 3. The deviceof claim 1, wherein the second electrode extends from within the firstelectrode through an aperture in the first electrode.
 4. The device ofclaim 1, wherein the catheter is dimensioned to be insertable into abronchoscope comprising a side-facing ultrasound probe.
 5. The device ofclaim 1, wherein the second electrode is constructed at least in partfrom a shape-memory material having a martensite configuration at afirst lower temperature, and an austenite configuration at a secondtemperature above body temperature, and wherein the second electrode isconfigured to adopt a first straight configuration while in themartensite configuration, and a bend or coil while in the austeniteconfiguration.
 6. The device of claim 1, wherein the first and secondelectrodes comprise a bipolar radiofrequency ablation electrode.
 7. Thedevice of claim 1, further comprising a fluid source connected to thecatheter and in fluid communication with at least one of the first orsecond electrodes.
 8. A system for the delivery of energy to a region oflung tissue, the system comprising: an energy delivery devicecomprising: a catheter configured to be inserted into an airway, thecatheter comprising a first electrode and a second electrode; a handleattached at a proximal end of the catheter, the handle comprising afirst activation toggle configured to extend the second electrode from achannel enclosed by the first electrode and the catheter, wherein thesecond electrode is received in a movable manner within the channel ofthe first electrode, wherein the second electrode is extendable from adistal end of the first electrode to form a first extendedconfiguration, wherein the second electrode is in a first configurationwhen within the first electrode, wherein when a distal end of the secondelectrode extends distally from the first electrode, a portion of thesecond electrode that is extended from the first electrode transitionsto a second configuration; and a power source connected to the firstelectrode and the second electrode via first and second electricalleads, the power source configured to deliver RF energy; and a conduitinsertable into an airway and selected from the group consisting of abronchoscope and a guide sheath, the catheter being insertable andmovable therein, wherein when in the first configuration the secondelectrode conforms to the first electrode, wherein the secondconfiguration is at least one of a helical or a coiled configuration,wherein the first configuration is not one of a helical or a coiledconfiguration.
 9. The system of claim 8, further comprising a fluidsource connected to the device and configured to deliver fluid out of adistal end of the catheter.
 10. A device for the delivery of energy to aregion of lung tissue, the device comprising: a guide sheath; a catheterconfigured to be inserted into the guide sheath, the catheter comprisesa distal section, the distal section comprises a first electrode,wherein the first electrode and the catheter are hollow having a channelenclosed by the first electrode and the catheter, wherein a distal endof the distal section comprises a piercing tip configured to piercethrough an airway wall; and a second electrode received in a movablemanner within the channel of the first electrode, wherein the secondelectrode is extendable independent from the first electrode, whereinthe second electrode extends proximally from the piercing tip to form acoil, wherein the device comprises: a pre-tissue piercing configuration,wherein the second electrode is positioned within the channel of thefirst electrode and the first electrode is positioned within the guidesheath, wherein a configuration of the second electrode conforms to thecatheter; a tissue piercing configuration, wherein the second electrodeis positioned within the first electrode and the first electrode isextended beyond a distal end of the guide sheath; and an energy deliveryconfiguration, wherein the first electrode is extended beyond the distalend of the guide sheath and the second electrode is extended beyond thepiercing tip, wherein a portion of the second electrode that is extendedfrom the piercing tip changes from the configuration of the catheter toa second configuration, wherein the second configuration comprises ahelical configuration, wherein the catheter is not in a helicalconfiguration when in the pre-tissue piercing configuration and in thetissue piercing configuration.